Product Details

SNP ID
rs45498595
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:50977213 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACTCCTGCCAACTCTGCACCCCAC[C/G]ACGGCTGGCTGAGCTCCTTGCTGTG
Phenotype
MIM: 606555
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TRIM9 PubMed Links

Gene Details

Gene
TRIM9
Gene Name
tripartite motif containing 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015163.5 3593 UTR 3 NP_055978.4
NM_052978.4 3593 Intron NP_443210.1
XM_005267301.3 3593 UTR 3 XP_005267358.1
XM_005267302.3 3593 UTR 3 XP_005267359.1
XM_006720018.3 3593 UTR 3 XP_006720081.1
XM_011536389.2 3593 Intron XP_011534691.1
XM_017020943.1 3593 UTR 3 XP_016876432.1
XM_017020944.1 3593 UTR 3 XP_016876433.1
XM_017020945.1 3593 UTR 3 XP_016876434.1
XM_017020946.1 3593 UTR 3 XP_016876435.1
XM_017020947.1 3593 UTR 3 XP_016876436.1
XM_017020948.1 3593 UTR 3 XP_016876437.1
XM_017020949.1 3593 UTR 3 XP_016876438.1
XM_017020950.1 3593 UTR 3 XP_016876439.1

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